NDC 0440-7128

ATORVASTATIN CALCIUM

Atorvastatin Calcium

ATORVASTATIN CALCIUM is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Liberty Pharmaceuticals, Inc.. The primary component is Atorvastatin Calcium Propylene Glycol Solvate.

Product ID0440-7128_6bd17203-4f17-48d0-a5c9-b80e0df8cdf5
NDC0440-7128
Product TypeHuman Prescription Drug
Proprietary NameATORVASTATIN CALCIUM
Generic NameAtorvastatin Calcium
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2012-05-29
Marketing CategoryANDA / ANDA
Application NumberANDA090548
Labeler NameLiberty Pharmaceuticals, Inc.
Substance NameATORVASTATIN CALCIUM PROPYLENE GLYCOL SOLVATE
Active Ingredient Strength80 mg/1
Pharm ClassesHMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 0440-7128-90

90 TABLET, FILM COATED in 1 BOTTLE (0440-7128-90)
Marketing Start Date2012-05-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0440-7128-90 [00440712890]

ATORVASTATIN CALCIUM TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090548
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-05-29
Inactivation Date2020-01-31

NDC 0440-7128-60 [00440712860]

ATORVASTATIN CALCIUM TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090548
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-05-29
Inactivation Date2020-01-31

NDC 0440-7128-85 [00440712885]

ATORVASTATIN CALCIUM TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090548
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-05-29
Inactivation Date2020-01-31

NDC 0440-7128-30 [00440712830]

ATORVASTATIN CALCIUM TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090548
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-05-29
Inactivation Date2020-01-31

NDC 0440-7128-81 [00440712881]

ATORVASTATIN CALCIUM TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090548
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-05-29
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ATORVASTATIN CALCIUM PROPYLENE GLYCOL SOLVATE80 mg/1

OpenFDA Data

SPL SET ID:fdfba989-7618-44ec-9ce1-8bff97c4a646
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 259255
  • Pharmacological Class

    • HMG-CoA Reductase Inhibitor [EPC]
    • Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

    NDC Crossover Matching brand name "ATORVASTATIN CALCIUM" or generic name "Atorvastatin Calcium"

    NDCBrand NameGeneric Name
    67877-514Atorvastatin CalciumAtorvastatin Calcium
    67877-512Atorvastatin CalciumAtorvastatin Calcium
    67877-511Atorvastatin CalciumAtorvastatin Calcium
    67877-513Atorvastatin CalciumAtorvastatin Calcium
    68071-1898Atorvastatin CalciumAtorvastatin Calcium
    68071-1551Atorvastatin CalciumAtorvastatin Calcium
    68071-1886ATORVASTATIN CALCIUMATORVASTATIN CALCIUM
    68071-1695ATORVASTATIN CALCIUMATORVASTATIN CALCIUM
    68071-1553ATORVASTATIN CALCIUMATORVASTATIN CALCIUM
    68071-1556Atorvastatin CalciumAtorvastatin Calcium
    68071-3267ATORVASTATIN CALCIUMATORVASTATIN CALCIUM
    68071-1885ATORVASTATIN CALCIUMATORVASTATIN CALCIUM
    68071-1915Atorvastatin CalciumAtorvastatin Calcium
    68071-2018ATORVASTATIN CALCIUMATORVASTATIN CALCIUM
    68071-3399Atorvastatin CalciumAtorvastatin Calcium
    68071-3374Atorvastatin CalciumAtorvastatin Calcium
    68071-3047Atorvastatin CalciumAtorvastatin Calcium
    68071-4179ATORVASTATIN CALCIUMATORVASTATIN CALCIUM
    68071-4171Atorvastatin CalciumAtorvastatin Calcium
    68071-4287Atorvastatin CalciumAtorvastatin Calcium
    68071-3167Atorvastatin CalciumAtorvastatin Calcium
    68071-4136Atorvastatin CalciumAtorvastatin Calcium
    68071-4302ATORVASTATIN CALCIUMATORVASTATIN CALCIUM
    68071-4308ATORVASTATIN CALCIUMATORVASTATIN CALCIUM
    68071-4472Atorvastatin CalciumAtorvastatin Calcium
    68071-4267ATORVASTATIN CALCIUMATORVASTATIN CALCIUM
    68071-4336ATORVASTATIN CALCIUMATORVASTATIN CALCIUM
    68071-4150Atorvastatin CalciumAtorvastatin Calcium
    68071-3371Atorvastatin CalciumAtorvastatin Calcium
    68071-4185Atorvastatin CalciumAtorvastatin Calcium
    68071-4396ATORVASTATIN CALCIUMATORVASTATIN CALCIUM
    68071-4279Atorvastatin CalciumAtorvastatin Calcium
    68071-4506Atorvastatin CalciumAtorvastatin Calcium
    68071-4220Atorvastatin CalciumAtorvastatin Calcium
    68071-4797ATORVASTATIN CALCIUMATORVASTATIN CALCIUM
    68071-4301ATORVASTATIN CALCIUMATORVASTATIN CALCIUM
    68071-4798ATORVASTATIN CALCIUMATORVASTATIN CALCIUM
    68071-4480Atorvastatin CalciumAtorvastatin Calcium
    68084-098ATORVASTATIN CALCIUMATORVASTATIN CALCIUM
    68084-099ATORVASTATIN CALCIUMATORVASTATIN CALCIUM
    68071-4806Atorvastatin CalciumAtorvastatin Calcium
    68071-4654Atorvastatin CalciumAtorvastatin Calcium
    68084-097ATORVASTATIN CALCIUMATORVASTATIN CALCIUM
    68084-590ATORVASTATIN CALCIUMATORVASTATIN CALCIUM
    0440-7128ATORVASTATIN CALCIUMATORVASTATIN CALCIUM
    68151-1013ATORVASTATIN CALCIUMATORVASTATIN CALCIUM
    68258-6993Atorvastatin CalciumAtorvastatin Calcium
    68258-6042Atorvastatin CalciumAtorvastatin Calcium
    68258-6044Atorvastatin CalciumAtorvastatin Calcium
    68258-6043Atorvastatin CalciumAtorvastatin Calcium

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